Overview
Ida Paramonov practices practicing medicine in Barcelona, Spain.
Her clinical expertise encompasses Hereditary Ataxia, Spinal Muscular Atrophy (SMA), Mosaicism, and X-Linked Agammaglobulinemia.
She is actively involved in clinical research, co-authoring 31 peer reviewed articles.
Gender
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Ida Paramonov
Is Ida Paramonov a top-rated expert for Hereditary Ataxia?
MediFind is an objective health platform that identifies experts based on real-world data. Ida Paramonov is classified as an Experienced expert for Hereditary Ataxia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Ida Paramonov participate in research or clinical trials?
Yes. Ida Paramonov has published 31 articles and abstracts on conditions like Hereditary Ataxia. You can view a list of Ida Paramonov's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Experienced
- Ciliary Dyskinesia-BronchiectasisMs. Paramonov isExperienced. Learn about Ciliary Dyskinesia-Bronchiectasis.
- Common Variable Immune DeficiencyMs. Paramonov isExperienced. Learn about Common Variable Immune Deficiency.
- Congenital HypothyroidismMs. Paramonov isExperienced. Learn about Congenital Hypothyroidism.
- DextrocardiaMs. Paramonov isExperienced. Learn about Dextrocardia.
- Dextrocardia with Situs InversusMs. Paramonov isExperienced. Learn about Dextrocardia with Situs Inversus.
- Drug Induced DyskinesiaMs. Paramonov isExperienced. Learn about Drug Induced Dyskinesia.
- EpilepsyMs. Paramonov isExperienced. Learn about Epilepsy.
- Hereditary AtaxiaMs. Paramonov isExperienced. Learn about Hereditary Ataxia.
- Kartagener SyndromeMs. Paramonov isExperienced. Learn about Kartagener Syndrome.
- Leber Hereditary Optic Neuropathy (LHON)Ms. Paramonov isExperienced. Learn about Leber Hereditary Optic Neuropathy (LHON).
- Marfan SyndromeMs. Paramonov isExperienced. Learn about Marfan Syndrome.
- MosaicismMs. Paramonov isExperienced. Learn about Mosaicism.
- Neonatal HypothyroidismMs. Paramonov isExperienced. Learn about Neonatal Hypothyroidism.
- Primary Lateral SclerosisMs. Paramonov isExperienced. Learn about Primary Lateral Sclerosis.
- Situs InversusMs. Paramonov isExperienced. Learn about Situs Inversus.
- Spinal Muscular Atrophy (SMA)Ms. Paramonov isExperienced. Learn about Spinal Muscular Atrophy (SMA).
- X-Linked AgammaglobulinemiaMs. Paramonov isExperienced. Learn about X-Linked Agammaglobulinemia.